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About This Item

 

Full Description



Cross References:
ISO 9001
ISO 11135-1
ISO 11137-1
ISO 11137-2
ISO 13408-2
ISO 13408-3
ISO 13408-4
ISO 13408-5
ISO 13408-6
ISO 13485
ISO 14160
ISO 14644-1:1999
ISO 14644-2
ISO 14644-3
ISO 14644-4
ISO 14644-5
ISO 14644-7
ISO 14698-1
ISO 14698-2
ISO 14937
ISO 14971
ISO 17665-1
ISO 20857
ICH Guidance for Industry - Q9 Quality Risk Management
ISO 9000:2005
ISO 9004
ISO 11137-3
ISO/TS 11139
ISO/TR 14969
ISO 13485:2003
ISO 15223
ANSI/AAMI ST67:2003
IEC 60812
EN 556-2
EN 1822-1
90/385/EEC
93/42/EEC
98/79/EC


Incorporates the following:
Amendment, June 2013. Amends and replaces BS EN ISO 13408-1:2011
 

Document History

  1. BS EN ISO 13408-1:2024


    Aseptic processing of health care products-General requirements

    • Most Recent
  2. BS EN ISO 13408-1:2015


    Aseptic processing of health care products-General requirements

    • Historical Version
  3. BS EN ISO 13408-1:2011+A1:2013

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    Aseptic processing of health care products-General requirements

    • Historical Version
  4. BS EN ISO 13408-1:2011


    Aseptic processing of health care products. General requirements

    • Historical Version
  5. BS 07/30090385 DC


    ISO 13408-1. Aseptic processing of health care products. Part 1. General requirements

    • Historical Version
  6. BS EN 13824:2004


    Sterilization of medical devices. Aseptic processing of liquid medical devices. Requirements

    • Historical Version